List of variants in gene LMNB2 reported as benign by Athena Diagnostics Inc

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 5

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HGVS	dbSNP	gnomAD frequency
NM_032737.4(LMNB2):c.704G>A (p.Arg235Gln)	rs121912497	0.01005
NM_032737.4(LMNB2):c.804C>T (p.Asp268=)	rs150969746	0.00159
NM_032737.4(LMNB2):c.1554G>C (p.Thr518=)	rs11882908
NM_032737.4(LMNB2):c.402C>T (p.Ser134=)	rs148213507
NM_032737.4(LMNB2):c.912C>A (p.Arg304=)	rs202001996

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